HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796191Generated: October 31, 2026
4-Nitrophenol → Ethyl 4-nitrophenyl carbonate
https://huagongshe.com/reaction/1796191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-nitrophenyl carbonate | HCID 586863 | 95% |
Reaction Steps
To a solution of 4-nitrophenol (1.00 g) in dichloromethane (20 ml) were added dropwise ethyl chloroformate (0.70 ml) and pyridine (0.70 ml) under ice-cooling, and the resulting mixture was stirred at room temperature overnight and then evaporated in vacuo. To the residue obtained was added ethyl acetate, and the organic layer was washed successively with a saturated aqueous sodium hydrogencarbonate solution, a saturated aqueous sodium chloride solution, a saturated aqueous potassium hydrogensulfate solution and a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and evaporated in vacuo. The residual solid obtained was collected by filtration using hexane to afford ethyl 4-nitrophenyl carbonate (1.44 g, yield: 95%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030138B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-1f796e95d6c7409b88e9c4087a261aa3 |
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| Source note | uspto-grants-2006_04 |
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